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CAS 33224-01-0

:

trans-4-cotininecarboxylic acid

Description:
Trans-4-cotininecarboxylic acid is an organic compound characterized by its structural features derived from cotinine, a natural alkaloid found in tobacco. It possesses a carboxylic acid functional group, which contributes to its acidic properties and solubility in polar solvents. The "trans" configuration indicates that the substituents around the double bond in the cyclohexane ring are positioned opposite to each other, influencing its stereochemistry and potentially its biological activity. This compound is of interest in medicinal chemistry and pharmacology due to its structural similarity to nicotine and its potential effects on the central nervous system. Additionally, trans-4-cotininecarboxylic acid may exhibit various chemical reactivity patterns typical of carboxylic acids, such as undergoing esterification or decarboxylation under specific conditions. Its CAS number, 33224-01-0, allows for precise identification in chemical databases and literature. Overall, trans-4-cotininecarboxylic acid represents a significant compound for research in tobacco-related studies and its derivatives.
Formula:C11H12N2O3
InChI:InChI=1/C11H12N2O3/c1-13-9(14)5-8(11(15)16)10(13)7-3-2-4-12-6-7/h2-4,6,8,10H,5H2,1H3,(H,15,16)/t8-,10+/m1/s1
Synonyms:
  • trans-1-Methyl-4-carboxy-5-(3-pyridyl)-2-pyrrolidinone
  • (2S,3S)-1-methyl-5-oxo-2-(pyridin-3-yl)pyrrolidine-3-carboxylic acid
  • (2R,3R)-1-methyl-5-oxo-2-(3-pyridyl)pyrrolidine-3-carboxylic acid
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